Yazar "Ceylaner, Serdar" için listeleme
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First case of MELAS syndrome presenting with local brain edema requiring decompressive craniectomy
Yeşilbaş, Osman; Şengenç, Esma; Ersoy Olbak, Melike; Bako, Derya; Nizam, Öznur Gökçe; Seyithanoğlu, Mehmet Hakan; Pehlivan, Davut; Ceylaner, Serdar; İçağasıoğlu, Dilara; Aydın, Kürşad (Turkish Neurosurgical Society, 2022)Mitochondrial encephalomyopathy, lactic acidosis, and recurrent stroke-like episodes (MELAS) syndrome is a rare but one of the most common maternally inherited multisystem disorder. Although patients with MELAS present a ... -
Hypomyelination and congenital cataract: Three siblings presentation
Karalök, Zeynep Selen; Gürkaş Esra; Aydın, Kürşad; Ceylaner, Serdar (Wolters Kluwer Medknow Publications, 2020)Hypomyelination and congenital cataract (HCC) is a condition, which is caused by mutations in the FAM126A gene and is characterized by congenital cataract, progressive neurologic impairment, and myelin deficiency in both ... -
Stimulus-induced myoclonus treated effectively with clonazepam in genetically confirmed Coffin-Lowry syndrome
Arslan, Elif Bengi; Ceylaner, Serdar; Turanlı, Güzide (Elsevier, 2014)Purpose: Coffin-Lowry syndrome (CLS) is a rare X-linked semidominant syndromic genetic disorder that is characterized by typical facial and radiologic findings, psychomotor and growth retardation, and various skeletal ...